FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MONARCH II IOL DELIVERY SYSTEM

K Number: K001157 · Decision Jun 27, 2000
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
38
Applicant Total
14
Review Days
78

Basic Information

Device Name
MONARCH II IOL DELIVERY SYSTEM
K Number
K001157
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ALCON RESEARCH, LTD.
Date Received
April 10, 2000
Decision Date
June 27, 2000
Product Code
KYB
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KYB Lens, Guide, Intraocular

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